List of variants in gene combination MIR4709, NPC2 reported as uncertain significance for immune system disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006432.5(NPC2):c.*86G>A	rs146900446	0.00002
NM_006432.5(NPC2):c.*115C>T	rs780515697	0.00001

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